Adverse Event Reporting Jobs (NOW HIRING)

... adverse event reporting, and quality analytics. • Integrate data from multiple systems, including Oracle and quality management platforms. • Create documentation for workflows, data logic, and ...

Provides medical evaluation of adverse event reports * Performs various tasks in support of clinical research including the reporting, collecting, and sharing of results and issues around adverse ...

Support the preparation, review, and submission of adverse event reports to regulatory authorities as required. * Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs ...

Support the preparation, review, and submission of adverse event reports to regulatory authorities as required. * Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs ...

Ensures compliance with TRI Standard Operating Procedures, Food and Drug Administration and World Health Organization regulations and global regulations for the reporting of adverse events to ...

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

The PL role reports into the Global Process Owner (GPO) who is accountable to provide high-level ... Every adverse event we capture more accurately, every process we automate with precision, every AI ...

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

The PL role reports into the Global Process Owner (GPO) who is accountable to provide high-level ... Every adverse event we capture more accurately, every process we automate with precision, every AI ...

The PL role reports into the Global Process Owner (GPO) who is accountable to provide high-level ... Every adverse event we capture more accurately, every process we automate with precision, every AI ...

Mundelein, IL 60060 (HYBRID, 3 Day Onsite and 2 Day Remote) Pay Range: $28/hr - $30/hr Must Haves: 5+ years of experience in complaint handling, adverse event reporting, MDR evaluation, post-market ...

Bachelor's degree in Life Sciences, Regulatory Affairs, Biomedical Engineering, Healthcare, or a related field 5+ years of experience in complaint handling, adverse event reporting, MDR evaluation ...

Adverse Event Reporting - the investigation and reporting of medical product experiences, in depth investigation of medical adverse events and works with Medical Affairs, Clinical, and Regulatory ...

Reviewing adverse event reports for completeness and accuracy * Communicating with partners or affiliates when clarification is needed * Performing duplicate searches * Entering initial case data